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CAS 958451-72-4

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B-[4-(Difluoromethoxy)-3-methylphenyl]boronic acid

Description:
B-[4-(Difluoromethoxy)-3-methylphenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a difluoromethoxy group and a methyl group, contributing to its unique electronic and steric properties. The difluoromethoxy group enhances the compound's lipophilicity and may influence its reactivity and interaction with biological targets. Boronic acids are often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Additionally, the presence of the boron atom allows for potential applications in drug development, particularly in the design of inhibitors for certain enzymes. Overall, this compound exemplifies the versatility of boronic acids in both synthetic and pharmaceutical chemistry.
Formula:C8H9BF2O3
InChI:InChI=1S/C8H9BF2O3/c1-5-4-6(9(12)13)2-3-7(5)14-8(10)11/h2-4,8,12-13H,1H3
InChI key:InChIKey=HNSXGLPRKOFDNV-UHFFFAOYSA-N
SMILES:O(C(F)F)C1=C(C)C=C(B(O)O)C=C1
Synonyms:
  • B-[4-(Difluoromethoxy)-3-methylphenyl]boronic acid
  • [4-(Difluoromethoxy)-3-methylphenyl]boronic acid
  • boronic acid, B-[4-(difluoromethoxy)-3-methylphenyl]-
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